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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364402Generated: October 30, 2026

N-(2-Aminoethyl)ethyleneurea → HCID 69480462, compound

https://huagongshe.com/reaction/2364402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)ethyleneureaHCID 80480—
ReactantSodium BisulfateHCID 516919—
Reactantethyl 1-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylateHCID 69480967—
SolventEthanolHCID 702—
ProductHCID 69480462HCID 69480462—

Reaction Steps

A solution of ethyl 1-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate (0.025 g, 0.049 mmol) in EtOH (1 mL) under nitrogen was treated with 1-(2-aminoethyl)-2-imidazolidinone (0.0078 g, 0.03 mmol, 50% W/W in IPA) for 30 min. (150° C. The reaction was further microwaved for 30 min.@150° C. after the addition of an additional 0.6 equivalents (0.015 mL) of the amine, cooled to ambient temperature, and treated with 1N NaHSO4. The resulting suspension was filtered and the filtrate was concentrated in vacuo. The filtrate residue was purified by reversed phase HPLC. Pure fractions were combined and concentrated to afford the title compound as an off-white solid: ES+ MS: 469 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691991B2
Source datasetuspto-grants-2014_04
ORD IDord-95b18baa4a9f46dfb519d6b35975dd14
Source noteuspto-grants-2014_04